![Olean-12-en-28-oicacid, 3-[(O-6-deoxy-a-L-mannopyranosyl-(1®2)-O-[b-D-glucopyranosyl-(1®4)]-a-L-ar…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F343352-hederacolchiside-e.webp&w=3840&q=75)
CAS 33783-82-3: Olean-12-en-28-oicacid, 3-[(O-6-deoxy-a-L-mannopyranosyl-(1®2)-O-[b-D-glucopyranosyl-(1®4)]-a-L-arabinopyranosyl)oxy]-, O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b)-
Formula:C65H106O30
InChI:InChI=1S/C65H106O30/c1-25-36(68)41(73)46(78)54(86-25)93-51-30(22-67)89-53(50(82)45(51)77)84-23-31-39(71)44(76)49(81)57(90-31)95-59(83)65-18-16-60(3,4)20-28(65)27-10-11-34-62(7)14-13-35(61(5,6)33(62)12-15-64(34,9)63(27,8)17-19-65)92-58-52(94-55-47(79)42(74)37(69)26(2)87-55)40(72)32(24-85-58)91-56-48(80)43(75)38(70)29(21-66)88-56/h10,25-26,28-58,66-82H,11-24H2,1-9H3/t25-,26-,28-,29+,30+,31+,32-,33-,34+,35-,36-,37-,38+,39+,40-,41+,42+,43-,44-,45+,46+,47+,48+,49+,50+,51+,52+,53+,54-,55-,56-,57-,58-,62-,63+,64+,65-/m0/s1
InChI key:InChIKey=DXLORNSIGDEVQK-ORHSKWSZSA-N
SMILES:C(O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O[C@H]3[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O3)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O)(=O)[C@]45[C@](C=6[C@@](C)(CC4)[C@@]7(C)[C@](CC6)([C@]8(C)[C@@](CC7)(C(C)(C)[C@@H](O[C@H]9[C@H](O[C@H]%10[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O%10)[C@@H](O)[C@@H](O[C@@H]%11O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%11O)CO9)CC8)[H])[H])(CC(C)(C)CC5)[H]
Synonyms:- 3-O-α-<span class="text-smallcaps">L</smallcap>-Rhamnopyranosyl-(1→2)[β-<smallcap>D</smallcap>-glucopyranosyl(1→4)]-α-<smallcap>L</smallcap>-arabinopyranosoleanolic acid 28-α-<smallcap>L</smallcap>-rhamnopyranosyl-(1→4)-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)-β-<smallcap>D</span>-glucopyranoside
- 3b-[(O-b-D-Glucopyranosyl-(1® 4)-O-[a-L-rhamnopyranosyl-(1® 2)]-a-L-arabinopyranosyl)oxy]olean-18-en-28-oicacid O-a-L-rhamnopyranosyl-(1® 4)-O-b-D-glucopyranosyl-(1® 6)-b-D-glucopyranosyl ester
- 3β-[(O-β-<span class="text-smallcaps">D</smallcap>-Glucopyranosyl-(1→4)-O-[α-<smallcap>L</smallcap>-rhamnopyranosyl-(1→2)]-α-<smallcap>L</smallcap>-arabinopyranosyl)oxy]olean-18-en-28-oic acid O-α-<smallcap>L</smallcap>-rhamnopyranosyl-(1→4)-O-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)-β-<smallcap>D</span>-glucopyranosyl ester
- Hederacholchiside E
- Hederacolchiside E
- HederacolchisideE (8CI)
- Olean-12-en-28-oic acid, 3-[(O-6-deoxy-α-<span class="text-smallcaps">L</smallcap>-mannopyranosyl-(1→2)-O-[β-<smallcap>D</smallcap>-glucopyranosyl-(1→4)]-α-<smallcap>L</smallcap>-arabinopyranosyl)oxy]-, O-6-deoxy-α-<smallcap>L</smallcap>-mannopyranosyl-(1→4)-O-β-<smallcap>D</smallcap>-glucopyranosyl-(1→6)-β-<smallcap>D</span>-glucopyranosyl ester, (3β)-
- 3-O-α-L-Rhamnopyranosyl-(1→2)[β-D-glucopyranosyl(1→4)]-α-L-arabinopyranosoleanolic acid 28-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside
- Olean-12-en-28-oic acid, 3-[(O-6-deoxy-α-L-mannopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl)oxy]-, O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, (3β)-
- 3β-[(O-β-D-Glucopyranosyl-(1→4)-O-[α-L-rhamnopyranosyl-(1→2)]-α-L-arabinopyranosyl)oxy]olean-18-en-28-oic acid O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester
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Found 3 products.
Hederacolchiside E
CAS:Hederacolchiside E: antioxidant, neuroprotective in AD, reduces oxidative stress, inhibits lipid peroxidation.Formula:C65H106O30Purity:99.78%Color and Shape:SolidMolecular weight:1367.52Hederacolchiside E
CAS:Hederacolchiside E is a natural glycoside, which is a bioactive compound sourced primarily from plants such as those in the Araliaceae family. Glycosides like Hederacolchiside E are known for their complex structures, comprising sugar moieties glycosidically linked to a non-sugar aglycone component. In the context of Hederacolchiside E, its aglycone part is derived from hederagenin, a pentacyclic triterpenoid compound. The mode of action for Hederacolchiside E involves modulating the activity of various inflammatory mediators. It exerts effects on pathways related to cytokine production and cellular oxidative stress, which are critical in inflammatory responses. These biochemical interactions position Hederacolchiside E as a candidate for further studies in inflammation management. In terms of applications, Hederacolchiside E has been investigated primarily for its anti-inflammatory potential. Scientific research continues to examine its utility in pharmacological contexts, exploring its efficacy and safety in potential therapeutic roles. The compound's properties also invite interest in natural product chemistry and the development of plant-based medicinal agents. Continued exploration in this area contributes to a broader understanding of natural compounds and their integration into biomedical solutions.Formula:C65H106O30Purity:Min. 95%Molecular weight:1,367.52 g/mol
